Results 231 to 240 of about 54,323 (280)

Usual Interstitial Pneumonia

Seminars in Respiratory and Critical Care Medicine, 2001
Usual interstitial pneumonia (UIP) is a distinct histological lesion observed in idiopathic pulmonary fibrosis (IPF), but can be found in other etiologies. The diagnosis of UIP can be established by surgical lung biopsy or by high resolution thin section computed tomographic scans (provided the radiographic features are classical).
Lynch, J. P. III, Wurfel, M., Flaherty, Kevin R., White, Eric S., Martinez, Fernando J., Travis, William D., Raghu, G.   +6 more
openaire   +2 more sources

Usual and Desquamative Interstitial Pneumonia

Chest, 1976
all from the National H~~~ and L~~~ I~~~~~~, U.S, Public separately. Radiographic observations were recorded accordHealth Service. ing to the Bucharest ILO/UICC classification5 by two ob"Fogarty International Fellow, U.S. Public Health Service.
C B, Carrington, E A, Gaensler, R E, Coutu, M X, Fitzgerald, R G, Gupta   +4 more
openaire   +2 more sources

Utility of a Molecular Classifier as a Complement to HRCT to Identify Usual Interstitial Pneumonia.

American Journal of Respiratory and Critical Care Medicine, 2020
Rationale Usual interstitial pneumonia (UIP) is the defining morphology of idiopathic pulmonary fibrosis (IPF). Guidelines for IPF diagnosis conditionally recommend surgical lung biopsy (SLB) for histopathology diagnosis of UIP when radiology and ...
L. Richeldi, M. Scholand, David A. Lynch, Thomas V. Colby, Jeffrey L. Myers, S. Groshong, Jonathan H. Chung, S. Benzaquen, S. Nathan, J Russell Davis, Shelley L. Schmidt, L. Hagmeyer, D. Sonetti, J. Hetzel, Gerard J. Criner, A. Case, Murali Ramaswamy, K. Calero, U.A. Gauhar, Nina M Patel, L. Lancaster, Yoonha Choi, D. Pankratz, P. S. Walsh, L. Lofaro, Jing Huang, S. Bhorade, Giulia C. Kennedy, Fernando J. Martinez, G. Raghu   +29 more
semanticscholar   +1 more source

Deep Learning Classification of Usual Interstitial Pneumonia Predicts Outcomes.

American Journal of Respiratory and Critical Care Medicine
RATIONALE Computed tomography (CT) enables noninvasive diagnosis of usual interstitial pneumonia (UIP), but enhanced image analyses are needed to overcome the limitations of visual assessment.
S. Humphries, D. Thieke, D. Baraghoshi, Matthew Strand, J. Swigris, K. Chae, Hye Jeon Hwang, Andrea S Oh, Kevin R. Flaherty, A. Adegunsoye, R. Jablonski, Cathryn T. Lee, Aliya N. Husain, Jonathan H. Chung, M. Strek, David A. Lynch   +15 more
semanticscholar   +1 more source

Cryobiopsy for Identification of Usual Interstitial Pneumonia and Other Interstitial Lung Disease Features: Further Lessons from COLDICE, a Prospective Multi-Center Study.

American Journal of Respiratory and Critical Care Medicine, 2020
RATIONALE Transbronchial lung cryobiopsy (TBLC) is an emerging technique for interstitial lung disease (ILD) diagnosis. Good histopathologic agreement between TBLC and surgical lung biopsy (SLB) was demonstrated in the COLDICE Study, however diagnostic ...
W. Cooper, A. Mahar, J. Myers, C. Grainge, T. Corte, J. Williamson, M. Vallely, Simon Lai, Ellie Mulyadi, P. Torzillo, M. Phillips, E. Lau, G. Raghu, L. Troy   +13 more
semanticscholar   +1 more source

Idiopathic Interstitial Pneumonias: Usual Interstitial Pneumonia versus Nonspecific Interstitial Pneumonia

Proceedings of the American Thoracic Society, 2006
Diffuse parenchymal lung diseases (DPLDs) are a group of disorders that involve the space between the epithelial and endothelial basement membranes. Recent guidelines for the classification of DPLDs recommended separating patients into several categories, including (1) DPLDs of known cause, (2) granulomatous DPLDs, (3) rare DPLDs with well-defined ...
openaire   +2 more sources

[Usual interstitial pneumonia].

Revue medicale de Bruxelles, 2004
We report the case of a 49-year old woman with an idiopathic pulmonary fibrosis (IPF) initially diagnosed as a systemic lupus erythematosus. The IPF is an uncommon clinical entity with an estimated prevalence from 3 to 6 cases per 100,000 in the general population of the United States.
Hougardy, Jean-Michel, Ocmant, Annick, Place, Sammy, Remmelink, Myriam, Mascart, Françoise, Cogan, Elie   +5 more
openaire   +1 more source

Usual interstitial pneumonia as a stand-alone diagnostic entity: the case for a paradigm shift?

The Lancet Respiratory Medicine, 2023
M. Selman, A. Pardo, A. Wells
semanticscholar   +1 more source

Usual Interstitial Pneumonia Pattern in the Lower Lung Lobes as a Prognostic Factor in Idiopathic Pleuroparenchymal Fibroelastosis

Respiration, 2018
Background: Idiopathic pleuroparenchymal fibroelastosis (IPPFE) is a rare interstitial pneumonia that is characterized by stiffness in both the upper lobes and pleura, which is evident on high resolution computed tomography (HRCT) of the chest.
Motoyasu Kato, S. Sasaki, K. Kurokawa, Takahiro I Nakamura, T. Yamada, H. Sasano, Naoko Arano, Moegi Komura, H. Ihara, O. Nagashima, Satomi Shiota, F. Takahashi, Kazuhisa Takahashi   +12 more
semanticscholar   +1 more source

Usual Interstitial Pneumonia

2008
Idiopathic pulmonary fibrosis (IPF), the most common and severe among idiopathic interstitial pneumonias, has now been definitively recognized as a distinct clinical entity, defined in the American Thoracic Society/European Respiratory Society (ATS/ERS) consensus statement as a specific form of chronic fibrosing interstitial pneumonia limited to the ...
Marco Chilosi, Bruno Murer, Venerino Poletti   +2 more
openaire   +1 more source